Implementation Consultant

2 weeks ago

London, Greater London, United Kingdom Veeva Systems, Inc. Full time

As a key member of our Professional Services team, Veeva Systems is seeking an experienced consultant to join our team of experts in navigating customers through complex software implementation. The ideal candidate will have deep expertise in regulatory information management (RIM) and a passion for helping life sciences companies optimize their data and document management processes.

The Senior Consultant will be responsible for understanding our customers' global regulatory needs, translating requirements into solution design, and defining global strategies for deploying our cloud-based solution for managing regulatory information across the enterprise. This is a remote position within the EU/UK if a candidate is in close proximity to an airport and able to meet travel requirements.

Key Responsibilities

  • Lead software implementation projects at life sciences companies, ranging from the world's largest pharmaceutical companies to emerging biotechs.
  • Lead the solution design for implementation and use of the Vault Regulatory suite.
  • Lead configuration requirements workshops, design, prototype, configure, and document content solutions.
  • Program and project management, including resource planning, leading and motivating a cross-functional team.
  • Primary customer liaison managing communication between the project team, customer, and internal stakeholders.
  • Mentor project team and consultants, helping others improve their consulting skills.

Requirements

  • 8+ years experience working with life sciences or healthcare companies performing system implementation experience either as a consultant, business or IT representative.
  • In-depth knowledge of drug development processes and regulatory submissions.
  • Expert on life sciences compliance and computer systems validation requirements.
  • Ability to travel as required by the business.

Nice to Have

  • Direct experience with systems such as Veeva Vault, PAREXEL/ LIQUENT InSight, CSC Regulatory Tracker, ArisGlobal Register, OpenText, SharePoint, Documentum, FirstDoc/FirstPoint, NextDocs, CARA, Salesforce, Workday, Oracle, SAP, Lorenz Docubridge, Extedo eCTD Manager, Master Control, Trackwise, other regulatory information management or submission publishing systems.
  • Consulting experience, working with a major system integrator or software vendor.
  • Regulatory Affairs, Regulatory Operations or Pharmacovigilance background.
  • Knowledge of Pharmaceutical, Biotechnology, and/or Medical Device and Diagnostics regulatory processes, data and content.
  • PMP certification.
  • Execution experience with Agile methodology and/or ACP Certification.
  • Life Science, computer science, or related degree.
  • Fluency in one or more of the following languages: German, French, Spanish, Italian.

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. We offer a remote work environment and support your flexibility to work from home or in the office, so you can thrive in your ideal environment.

As an equal opportunity employer, Veeva is committed to fostering a culture of inclusion and growing a diverse workforce. Diversity makes us stronger. Gender, race, ethnicity, religion, politics, sexual orientation, age, disability and life experience shape us all into unique individuals.

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